Elisa Conti

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2014-2023
Publications (10 Years): 4

Top Topics

Nlrp Inflammasome

Top Venues

Pharmaceuticals (Basel, Switzerland)

Diagnostics (Basel, Switzerland)

Case reports in neurological medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Marina Saresella, Chiara Paola Zoia, Francesca La Rosa, Chiara Bazzini, Gessica Sala, Erica Grassenis, Ivana Marventano, Ambra Hernis, Federica Piancone, Elisa Conti, Silvia Sesana, Francesca Re, Pierfausto Seneci, Carlo Ferrarese, Mario Salvatore Clerici
Glibenclamide-Loaded Engineered Nanovectors (GNVs) Modulate Autophagy and NLRP3-Inflammasome Activation. Pharmaceuticals (Basel, Switzerland) 16 (12) (2023)
Marina Saresella, Chiara Paola Zoia, Francesca La Rosa, Chiara Bazzini, Gessica Sala, Erica Grassenis, Ivana Marventano, Ambra Hernis, Federica Piancone, Elisa Conti, Silvia Sesana, Francesca Re, Pierfausto Seneci, Carlo Ferrarese, Mario Salvatore Clerici
Glibenclamide-Loaded Engineered Nanovectors (GNVs) Modulate Autophagy and NLRP3-Inflammasome Activation. Pharmaceuticals (Basel, Switzerland) 16 (12) (2023)
Francesca La Rosa, Chiara Paola Zoia, Chiara Bazzini, Alessandra Bolognini, Marina Saresella, Elisa Conti, Carlo Ferrarese, Federica Piancone, Ivana Marventano, Daniela Galimberti, Chiara Fenoglio, Elio Scarpini, Mario Clerici
Modulation of MAPK- and PI3/AKT-Dependent Autophagy Signaling by Stavudine (D4T) in PBMC of Alzheimer's Disease Patients. Cells 11 (14) (2022)
Federica Angiulli, Elisa Conti, Chiara Paola Zoia, Fulvio Da Re, Ildebrando Appollonio, Carlo Ferrarese, Lucio Tremolizzo
Blood-Based Biomarkers of Neuroinflammation in Alzheimer's Disease: A Central Role for Periphery? Diagnostics (Basel, Switzerland) 11 (9) (2021)
Lucio Tremolizzo, Gessica Sala, Elisa Conti, Virginia Rodriguez-Menendez, Antonella Fogli, Angela Michelucci, Paolo Simi, Silvana Penco, Christian Lunetta, Massimo Corbo, Carlo Ferrarese
Valproate Treatment in an ALS Patient Carrying a c.194G>A Spastin Mutation and SMN2 Homozygous Deletion. Case reports in neurological medicine 2014 (2014)